PrP aggregation can be seeded by pre-formed recombinant PrP amyloid fibrils without the replication of infectious prions

Dura mater is a potential source of Aβ seeds

(2016) Gabor G. Kovacs et al.   ACTA NEUROPATHOLOGICA

New Molecular Insight into Mechanism of Evolution of Mammalian Synthetic Prions

(2016) Natallia Makarava et al.   AMERICAN JOURNAL OF PATHOLOGY

Amyloid-β pathology and cerebral amyloid angiopathy are frequent in iatrogenic Creutzfeldt-Jakob disease after dural grafting

(2016) K Frontzek et al.   SWISS MEDICAL WEEKLY

Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases

(2016) Laura Pirisinu et al.   Scientific Reports

Propagation of Aß pathology: hypotheses, discoveries, and yet unresolved questions from experimental and human brain studies

(2015) Yvonne S. Eisele et al.   ACTA NEUROPATHOLOGICA

Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy

(2015) Zane Jaunmuktane et al.   NATURE

Synthetic Scrapie Infectivity: Interaction between Recombinant PrP and Scrapie Brain-Derived RNA

(2015) Steve Simoneau et al.   Virulence

A systematic investigation of production of synthetic prions from recombinant prion protein

(2015) Christian Schmidt et al.   Open Biology

Prion Protein-Specific Antibodies that Detect Multiple TSE Agents with High Sensitivity

(2014) Sandra McCutcheon et al.   PLoS One

Distinct synthetic A  prion strains producing different amyloid deposits in bigenic mice

(2014) J. Stohr et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Seeded strain-like transmission of β-amyloid morphotypes in APP transgenic mice

(2013) Götz Heilbronner et al.   EMBO REPORTS

Dissociation of Prion Protein Amyloid Seeding from Transmission of a Spongiform Encephalopathy

(2013) P. Piccardo et al.   JOURNAL OF VIROLOGY

Structural and functional characterization of two alpha-synuclein strains

(2013) Luc Bousset et al.   Nature Communications

Evaluation of Potential Infectivity of Alzheimer and Parkinson Disease Proteins in Recipients of Cadaver-Derived Human Growth Hormone

(2013) David J. Irwin et al.   JAMA Neurology

Stabilization of a Prion Strain of Synthetic Origin Requires Multiple Serial Passages

(2012) Natallia Makarava et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

A New Mechanism for Transmissible Prion Diseases

(2012) N. Makarava et al.   JOURNAL OF NEUROSCIENCE

Isolation of Novel Synthetic Prion Strains by Amplification in Transgenic Mice Coexpressing Wild-Type and Anchorless Prion Proteins

(2012) G. J. Raymond et al.   JOURNAL OF VIROLOGY

Purified and synthetic Alzheimer's amyloid beta (A ) prions

(2012) J. Stohr et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Mechanism of PrP-Amyloid Formation in Mice Without Transmissible Spongiform Encephalopathy

(2011) Martin Jeffrey et al.   BRAIN PATHOLOGY

De novo induction of amyloid-β deposition in vivo

(2011) R Morales et al.   MOLECULAR PSYCHIATRY

Prion-like acceleration of a synucleinopathy in a transgenic mouse model

(2011) Anne-Laure Mougenot et al.   NEUROBIOLOGY OF AGING

Prion-like propagation of mutant superoxide dismutase-1 misfolding in neuronal cells

(2011) Christian Münch et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Genesis of Mammalian Prions: From Non-infectious Amyloid Fibrils to a Transmissible Prion Disease

(2011) Natallia Makarava et al.   PLoS Pathogens

Cellular and sub-cellular pathology of animal prion diseases: relationship between morphological changes, accumulation of abnormal prion protein and clinical disease

(2010) Martin Jeffrey et al.   ACTA NEUROPATHOLOGICA

Recombinant prion protein induces a new transmissible prion disease in wild-type animals

(2010) Natallia Makarava et al.   ACTA NEUROPATHOLOGICA

Inverse Correlation of Thermal Lability and Conversion Efficiency for Five Prion Protein Polymorphic Variants

(2010) Louise Kirby et al.   BIOCHEMISTRY

Low Density Subcellular Fractions Enhance Disease-specific Prion Protein Misfolding

(2010) James F. Graham et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties

(2010) M. T. Bishop et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Peripherally Applied A -Containing Inoculates Induce Cerebral  -Amyloidosis

(2010) Y. S. Eisele et al.   SCIENCE

Protease-Sensitive Synthetic Prions

(2010) David W. Colby et al.   PLoS Pathogens

Transmission and spreading of tauopathy in transgenic mouse brain

(2009) Florence Clavaguera et al.   NATURE CELL BIOLOGY

Pathogenetical significance of porencephalic lesions associated with intracerebral inoculation of sheep with the bovine spongiform encephalopathy (BSE) agent

(2009) S. Sisó et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Design and construction of diverse mammalian prion strains

(2009) D. W. Colby et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Induction of cerebral  -amyloidosis: Intracerebral versus systemic A  inoculation

(2009) Y. S. Eisele et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Neuroinvasion in sheep transmissible spongiform encephalopathies: the role of the haematogenous route

(2008) S. Sisó et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY